B BRAUN MEDICAL INC recalls Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.

Recall date

July 9, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2176-2025

FDA classification

Class I

Brand / firm

B BRAUN MEDICAL INC

Sold / distributed

US distribution to AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NV, NY, OH, OR, PA, SC, SD, TN, TX, UT, VA, WA, WY. International distribution to Canada.

Why it was recalled

Label is incorrect. The product label indicates that the device contains an air eliminating filter. However, the filter utilized on this extension set is not indicated for removal of air and does not feature an air vent, which is common to air eliminating filters.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.